Translocator protein expression and localization in human endometrium and endometriosis: A potential target for a noninvasive diagnosis?

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Maíra Casalechi, Cynthia Dela Cruz, Wiviane A. Assis, Millene Vieira-Lopes, Felipe Eduardo F. Lopes, Antônio M.C. Francisco, Fernando M. Reis
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Abstract

The limitations of current imaging methods to detect small or superficial endometriotic lesions prompt the search for new molecular targets. TSPO is an 18 KDa protein located in the outer mitochondrial membrane, which can be traced by positron emission tomography (PET) using specific ligands. TSPO is located mostly in neurons and inflammatory sites outside the brain. We hypothesized that it might also be expressed in the human endometrium and endometrial-like tissue, being a target for molecular imaging of endometriosis. This prospective cross-sectional study included 28 women with endometriosis and 11 endometriosis-free controls. Endometriotic lesions (n = 49) and normal peritoneum (n = 13) from endometriosis patients were obtained during laparoscopy, while samples of eutopic endometrium from patients with endometriosis (n = 28) and from control women (n = 11) were collected in the operating room using a flexible device. TSPO mRNA expression was evaluated by quantitative reverse-transcription real-time PCR while protein expression was evaluated by immunohistochemistry with a monoclonal antibody antihuman TSPO. TSPO mRNA expression was detected in an invariable fashion in all tissue types evaluated; however, TSPO protein was found to be more abundant in the glandular epithelium than in the stroma, both in the endometrium and in the endometriotic lesions. Interestingly, hormone therapies did not alter the expression of TSPO, and its presence was mostly negative in tissues adjacent to endometriotic implants. As a proof of concept, the protein expression pattern of TSPO in endometriotic tissue and along the adjacent areas suggests that TSPO-based molecular imaging might be used for noninvasive endometriosis detection.

人类子宫内膜和子宫内膜异位症中转运蛋白的表达和定位:无创诊断的潜在目标?
目前的成像方法在检测小的或浅表的子宫内膜异位症病灶方面存在局限性,这促使人们寻找新的分子靶点。TSPO 是一种位于线粒体外膜的 18 KDa 蛋白质,可通过使用特定配体的正电子发射断层扫描(PET)对其进行追踪。TSPO 主要位于神经元和脑外炎症部位。我们假设它也可能在人类子宫内膜和子宫内膜样组织中表达,并成为子宫内膜异位症分子成像的靶点。这项前瞻性横断面研究包括 28 名患有子宫内膜异位症的妇女和 11 名无子宫内膜异位症的对照组妇女。子宫内膜异位症患者的子宫内膜异位病灶(49 例)和正常腹膜(13 例)是在腹腔镜手术中获得的,而子宫内膜异位症患者(28 例)和对照组妇女(11 例)的异位子宫内膜样本则是在手术室使用柔性装置收集的。TSPO mRNA 的表达通过反转录实时定量 PCR 进行评估,蛋白质的表达则通过抗人 TSPO 的单克隆抗体免疫组化进行评估。在所有接受评估的组织类型中,TSPO mRNA 的表达均无变化;但在子宫内膜和子宫内膜异位病变中,发现腺上皮的 TSPO 蛋白含量高于基质。有趣的是,激素疗法并不会改变 TSPO 的表达,而且在子宫内膜异位植入物附近的组织中,TSPO 的存在大多为阴性。作为概念验证,TSPO 在子宫内膜异位组织和邻近区域的蛋白表达模式表明,基于 TSPO 的分子成像可用于无创子宫内膜异位症检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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